Canonical Allele Identifier: CA360697499

Gene: SLC25A46

Linked Data

• MyVariant Identifiers: chr5:g.110097361A>T (hg19) ; chr5:g.110761661A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.110761661A>T , CM000667.2:g.110761661A>T	GRCh38
NC_000005.9:g.110097361A>T , CM000667.1:g.110097361A>T	GRCh37
NC_000005.8:g.110125260A>T	NCBI36
NG_051334.1:g.28526A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000355943.8:c.1136A>T MANE Select	ENSP00000348211.3:p.Glu379Val
ENST00000355943.7:c.1136A>T	ENSP00000348211.3:p.Glu379Val
ENST00000447245.6:c.893A>T	ENSP00000399717.2:p.Glu298Val
ENST00000504098.1:c.698A>T	ENSP00000425708.1:p.Glu233Val
ENST00000509432.1:c.497A>T	ENSP00000426604.1:p.Glu166Val
ENST00000513706.2:n.2736A>T
ENST00000513807.5:c.650A>T	ENSP00000421134.1:p.Glu217Val
NM_001303249.1:c.893A>T	NP_001290178.1:p.Glu298Val
NM_001303250.1:c.863A>T	NP_001290179.1:p.Glu288Val
NM_138773.2:c.1136A>T	NP_620128.1:p.Glu379Val
NM_001303249.2:c.893A>T	NP_001290178.1:p.Glu298Val
NM_001303250.2:c.863A>T	NP_001290179.1:p.Glu288Val
NM_138773.3:c.1136A>T	NP_620128.1:p.Glu379Val
NR_138151.1:n.1410A>T
NM_138773.4:c.1136A>T MANE Select	NP_620128.1:p.Glu379Val
NM_001303249.3:c.893A>T	NP_001290178.1:p.Glu298Val
NM_001303250.3:c.863A>T	NP_001290179.1:p.Glu288Val
NR_138151.2:n.1375A>T